Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2088-2021 — The Fresenius APD Luer-Lock Adapter, Catalog number 050-95018, is designed to connect a peritoneal dialysis bag equipped with a luer-lock connector to a Fresenius Automated Peritoneal Dialysis (APD) cycler set that uses the Fresenius Safe-Lock¿ connector (e.g., Liberty¿ cycler, Newton IQO cycler).

U.S. FDA — Device Enforcement · United States · 2021-04-28 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2088-2021
Date of alert: 2021-04-28
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Fresenius Medical Care Holdings, Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 00840861100811

Reported risk: Exposed to freezing temperatures due to refrigerated truck malfunctions

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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